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Terminology chevron_right Concepts chevron_right 128347007

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Component

128347007

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital anomaly of gastrointestinal tract (disorder)

Shortest Term

Gastrointestinal tract congenital anomaly

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Congenital anomaly of gastrointestinal tract (disorder)

SCTID: 128347007, Defined, Active

128347007|Congenital anomaly of gastrointestinal tract (disorder)|

en Congenital anomaly of gastrointestinal tract
en Congenital anomaly of gastrointestinal tract (disorder)
en Gastrointestinal tract congenital anomaly

Expression

128347007 |Congenital anomaly of gastrointestinal tract (disorder)|
 === 119292006 |Disorder of gastrointestinal tract (disorder)| + 
95470009 |Congenital anomaly of digestive tract (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 122865005 |Gastrointestinal tract structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
206637018 - Congenital anomaly of gastrointestinal tract (en) View
206637018	en	Synonym (core metadata concept)	Congenital anomaly of gastrointestinal tract	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
732328016 - Congenital anomaly of gastrointestinal tract (disorder) (en) View
732328016	en	Fully specified name (core metadata concept)	Congenital anomaly of gastrointestinal tract (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2475470013 - Gastrointestinal tract congenital anomaly (en) View
2475470013	en	Synonym (core metadata concept)	Gastrointestinal tract congenital anomaly	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (697482024) - 128347007 -> 122865005 (363698007) View
363698007 \|Finding site (attribute)\|	122865005 \|Gastrointestinal tract structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4971062027) - 128347007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4971063021) - 128347007 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4971064026) - 128347007 -> 122865005 (363698007) View
363698007 \|Finding site (attribute)\|	122865005 \|Gastrointestinal tract structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6096926028) - 128347007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10528076028) - 128347007 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10528077021) - 128347007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2590538023) - 128347007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3414059025) - 128347007 -> 122865005 (363698007) View
363698007 \|Finding site (attribute)\|	122865005 \|Gastrointestinal tract structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3414060024) - 128347007 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3619114028) - 128347007 -> 443341004 (116680003) View
116680003 \|Is a (attribute)\|	443341004 \|Congenital anomaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1756432022) - 128347007 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3181318020) - 128347007 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (163581029) - 128347007 -> 69518005 (116680003) View
116680003 \|Is a (attribute)\|	69518005 \|Congenital anomaly of digestive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1756433028) - 128347007 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1922024023) - 128347007 -> 95470009 (116680003) View
116680003 \|Is a (attribute)\|	95470009 \|Congenital anomaly of digestive tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (697483025) - 128347007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (163580028) - 128347007 -> 119292006 (116680003) View
116680003 \|Is a (attribute)\|	119292006 \|Disorder of gastrointestinal tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
95470009 View
95470009	Congenital anomaly of digestive tract (disorder)	Congenital digestive tract anomaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
119292006 View
119292006	Disorder of gastrointestinal tract (disorder)	Disease of gastrointestinal tract	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
720009004 View
720009004	Intractable diarrhea with choanal atresia and eye anomaly syndrome (disorder)	Tiêu chảy khó chữa kèm hẹp mũi sau và hội chứng bất thường mắt	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
253909006 View
253909006	Congenital gastrointestinal-urinary tract fistula (disorder)	Congenital gastrointestinal-urinary tract fistula	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
31686000 View
31686000	Congenital anomaly of lower alimentary tract (disorder)	Congenital abnormality of intestine	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
126764002 View
126764002	Congenital anomaly of intestinal tract (disorder)	Congenital anomaly of intestinal tract	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
33225004 View
33225004	Anorectal anomaly (disorder)	Anorectal anomaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
60699003 View
60699003	Congenital anomaly of stomach (disorder)	Congenital anomaly of stomach	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
69771008 View
69771008	Congenital anomaly of esophagus (disorder)	Dị tật bẩm sinh của thực quản	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (49139917-20d6-59d8-a8f9-5f1698621eff) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q45.9	TRUE	ALWAYS Q45.9	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|

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